What is Clinion eConsent?
Clinion eConsent is an electronic informed consent platform designed to digitize consent workflows for clinical trials. The platform enables participants to review, understand, and sign consent documents electronically through site-based or remote workflows. It supports consent version management, audit trails, investigator review, and EDC integration, helping sponsors, CROs, and research sites manage informed consent processes in a centralized and compliant environment.
Key Capabilities
Electronic Informed Consent - Enables participants to review and sign consent forms electronically using site-provided devices or their own devices, supporting both on-site and remote consent workflows.Remote and Site-Based Consent - Supports site eConsent, remote eConsent, and eConsent integrated with ePRO, providing flexibility across different study designs and participant engagement models.
Interactive Consent Experience - Supports multimedia content, embedded questions, and investigator interactions to help participants review study information and complete the consent process electronically.
Investigator Review and Approval - Allows investigators to review and approve consent forms electronically, reducing manual paperwork and supporting efficient participant onboarding.
ICF Version Control - Tracks consent form versions and supports re-consenting workflows for protocol amendments, helping ensure participants receive the latest approved consent documentation.
Automated Enrollment and EDC Integration - Integrates with Clinion EDC to support automatic subject enrollment and synchronized data flow between consent and study records.
Audit Trails and Compliance - Maintains time-stamped signatures, consent records, version histories, and audit trails to support regulatory requirements and inspection readiness.
Multilingual and Multi-Platform Support - Supports multilingual consent forms and access across smartphones, tablets, and web browsers, enabling use across diverse patient populations and geographic regions.
Key Benefits
- Digitized participant consent and enrollment workflows
- Support for remote and site-based consent models
- Centralized management of consent versions and re-consenting activities
- Reduced reliance on paper-based consent processes
- Automated enrollment through EDC integration
- Comprehensive audit trails and consent documentation
- Support for multilingual studies and global trial deployments
- Access across mobile, tablet, and web-based devices
Clinion eConsent is designed for sponsors, CROs, and research sites seeking to manage informed consent electronically, support remote trial models, maintain consent documentation, and streamline participant enrollment across Phase I–IV clinical trials.
Categories & Use Cases
Media
Screenshot of Dashboard | Clinion eConsent
